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1.
热力作用对烃源岩中重排藿烷类化合物形成的作用 总被引：1，自引：1，他引：0
通过对87个采自鄂尔多斯盆地煤系烃源岩和松辽盆地湖相烃源岩样品进行的地球化学分析结果显示,热力作用对烃源岩重排藿烷组成特征的影响强烈。随成熟度的变化,来自两套沉积体系的烃源岩中重排藿烷相对丰度的分布相似,随成熟度增大17α（H）-重排藿烷和18α（H）-新藿烷相对丰度均先增大后减小,并在Ro:0.80%~0.90%（生油窗）时达峰值。不同沉积环境的烃源岩中重排藿烷的成熟度与绝对浓度的变化规律一致。在Ro:0.50%~0.70%（未熟-低熟）阶段,重排藿烷绝对浓度较大;在Ro:0.70%~0.80%（成熟）阶段,重排藿烷的绝对浓度显著降低。不同沉积环境中重排藿烷的参数随成熟度的变化规律揭示:在重排藿烷的形成过程中,热力作用的影响要强于沉积环境和生物来源。 相似文献
2.
柴达木盆地北缘地区侏罗系（中下侏罗统）的优质烃源岩主要发育于湖相与三角洲相环境。研究了不同时代、不同沉积环境中烃源岩的生物标志物组成特征,结果发现,有3类化合物的分布与组成差异显著,包括三环萜烷（C19、C20、C21）的分布型式、重排藿烷的丰度以及规则甾烷的相对组成。其中,不同时代的差异主要体现在规则甾烷组成上;而不同沉积环境的差异主要体现为三环萜烷（C19、C20、C21）的分布型式及重排藿烷的丰度。分析认为,这些差异与烃源岩的沉积环境及其生源组成有密切关系。据此,初步将这些参数应用于两方面研究,一是为划分地层沉积环境提供“生物标志物相标志”,二是研究油源对比,取得良好效果。因此,本文研究结果具有重要实用价值与参考意义。 相似文献
3.
柴达木盆地北缘侏罗系不同沉积环境烃源岩生物标志物特征及其应用 总被引：2，自引：0，他引：2
柴达木盆地北缘地区侏罗系(中下侏罗统)的优质烃源岩主要发育于湖相与三角洲相环境。研究了不同时代、不同沉积环境中烃源岩的生物标志物组成特征,结果发现,有3类化合物的分布与组成差异显著,包括三环萜烷(C19、C20、C21)的分布型式、重排藿烷的丰度以及规则甾烷的相对组成。其中,不同时代的差异主要体现在规则甾烷组成上;而不同沉积环境的差异主要体现为三环萜烷(C19、C20、C21)的分布型式及重排藿烷的丰度。分析认为,这些差异与烃源岩的沉积环境及其生源组成有密切关系。据此,初步将这些参数应用于两方面研究,一是为划分地层沉积环境提供“生物标志物相标志”,二是研究油源对比,取得良好效果。因此,本文研究结果具有重要实用价值与参考意义。 相似文献
4.
塔里木阿瓦提凹陷乌鲁桥油苗地化特征及来源 总被引：1，自引：0，他引：1
阿瓦提凹陷乌鲁桥油苗全油碳同位素较重(-29.4‰)。在甲基菲分布分数图版上落在高成熟油区;甲基菲比值为2.03,高于塔里木盆地现已发现的高成熟凝析油和成熟度较高的原油,表明该油苗的成熟度高。萜烷、甾烷分布具有C29Ts、重排藿烷含量低,伽玛蜡烷丰度较高,中等—高丰度C28甾烷,低重排甾烷等分布特征。这与凹陷及其周缘的石炭系—二叠系、三叠系及中—上奥陶统这三套烃源岩的明显不同,而与寒武系烃源岩相似。综合分析认为乌鲁桥油苗来源于寒武系烃源岩成熟晚期阶段生成的烃类。 相似文献
5.
天草凹陷天2井油砂地球化学特征与油源研究 总被引：3，自引：1，他引：2
天草凹陷天2井油气显示丰富.以天2井油砂为剖析对象,采用定量色谱-质谱技术,从定性和定量两个角度精细剖析了油砂的生物标志物组合特征.油砂中C31～C35藿烷丰度依次降低,伽马蜡烷丰度较高,无重排藿烷和重排甾烷,C27～C29规则甾烷呈反"L"型分布,C28甾烷丰度较高.甾烷的异构化成熟度参数、甲基菲指数均显示油砂成熟度低.在对该区可能烃源岩生物标志物组合特征分析的基础上,从生物标志物指纹及其丰度特征确认了油砂与下白垩统巴音戈壁组下段烃源岩有成因联系,进一步明确了巴音戈壁组下段烃源岩为天草凹陷的主力烃源岩. 相似文献
6.
鄂尔多斯盆地东北部上古生界煤系烃源岩17α(H)-重排藿烷类的分布及成因探讨 总被引：3，自引：0，他引：3
鄂尔多斯盆地东北部上古生界10个典型煤系烃源岩样品中检测出三类重排藿烷,分别为17α(H)-重排藿烷、18α(H)-新藿烷以及未知结构的早洗脱重排藿烷。烃源岩样品中藿烷类具有两种分布型式:①以C30藿烷为主峰的C27~C35(缺C28)藿烷类常规分布型式,含少量17α (H)-重排藿烷和18α(H)-新藿烷;②以富含17α(H)-重排藿烷和C30早洗脱重排藿烷为特征。含有高~异常高相对丰度17α(H)-重排藿烷的烃源岩样品,其17α(H)-重排藿烷的绝对浓度也明显较高。从烃源岩生源构成、有机质丰度及其赋存状态、成熟度以及沉积与成岩环境4个方面探讨了高丰度17α(H)-重排藿烷的成因。研究结果表明,烃源岩中高丰度的17α(H)-重排藿烷的形成与高等植物生源有一定联系、亚氧化-氧化的扇缘泥炭沼泽相是形成高~异常高丰度17α(H)-重排藿烷的有利沉积相带;而烃源岩显微组分、有机质丰度及其赋存状态以及有机质成熟度的影响尚不确定。 相似文献
7.
柯克亚油田原油地球化学特征和油源研究 总被引：4，自引：0，他引：4
应用GC/MS、GC/MS/MS分析技术,剖析了塔西南地区侏罗系和二叠系两套烃源岩生物标志物组合特征,建立了区分的指标体系,即二叠系源岩重排藿烷、C30-未知萜烷含量丰富,侏罗系源岩重排藿烷含量较低,但检测到二萜类化合物,而在二叠系源岩中未检测到该类化合物。柯克亚原油重排藿烷、C30-未知萜烷发育。精细油-岩对比结果表明,柯克亚原油主要来源于二叠系烃源岩,同时原油中检测出微量的二萜类化合物,说明侏罗系烃源岩也有一定的贡献。 相似文献
8.
《地球化学》2017,(3)
以鄂尔多斯盆地陕北地区延长组下油层组烃源岩及储层抽提物为研究对象,探讨了17α(H)-重排藿烷和18α(H)-新藿烷系列化合物的分布规律、影响因素及在石油地质中的应用。鄂尔多斯盆地延长组湖相烃源岩普遍分布17α(H)-C_(30)重排藿烷(C_(30)DiaH),但研究区各层烃源岩之间C_(30)DiaH的相对丰度存在明显差异,深湖相缺氧环境的长7烃源岩相对丰度较低,而浅湖-半深湖相偏氧化环境的长7—长9黑色泥岩具有高-异常高的C_(30)DiaH。Ts、C29Ts、早洗脱重排藿烷与C_(30)DiaH之间表现出良好的正相关关系,说明在研究区重排藿烷类化合物可能与新藿烷系列具有相同的演化路径与形成机制。环境的氧化还原性和陆源的有机物来源等可能是制约17α(H)-重排藿烷相对丰度的主要因素,因此,不同油层组原油的17α(H)-重排藿烷相对丰度受到烃源岩的影响,用17α(H)-重排藿烷参数能很好地把研究区原油区分开来,为延长组不同油层的油源精细对比、油气富集规律和油气勘探提供可靠依据。 相似文献
9.
对北黄海盆地LV井中、上侏罗统烃源岩及上侏罗统原油（油砂抽提物）进行常规有机地球化学分析和碳同位素测试,分析研究烃源岩和原油的地球化学特征并探讨原油的来源问题。测试结果显示,侏罗系烃源岩达成熟-高熟阶段,有机质类型以Ⅲ型为主。中侏罗统烃源岩有机碳含量较高,但生烃潜能、氯仿沥青“A”及总烃含量低值,属于差的烃源岩。干酪根碳同位素总体偏重（-24.4‰～-23.5‰）,与原油碳同位素特征（-29‰左右）差异显著,排除与原油的母岩关系。上侏罗统烃源岩有机碳含量较中侏罗统低,但生烃潜能、氯仿沥青“A”及总烃含量高值。上侏罗统烃源岩抽提氯仿沥青“A”碳同位素（-26‰～-21.5‰）特征、单体烃碳同位素分布模式及甾萜烷生物标志物特征都与原油相似,综合分析认为原油应该来源于上侏罗统中干酪根类型较好、母质为混源的成熟烃源岩。 相似文献
10.
通过对富县地区延长组长6~长9原油及烃源岩的地球化学特征综合对比分析,认为研究区存在长7、长9两套有效烃源岩。长7烃源岩有机质类型为Ⅰ~Ⅱ1型,长9烃源岩的有机类型为Ⅱ1~Ⅱ2型。长7、长9烃源岩中Ts相对含量高于Tm,均达到成熟阶段。长7烃源岩五环三萜烷中C30藿烷丰度相对高于C29藿烷丰度,C30RH/C29Ts2,长7形成于还原环境;长9烃源岩中C30藿烷丰度与C29藿烷丰度基本相似,C30RH/C29Ts2,表明长9为弱氧化-弱还原环境。长6原油饱/芳比值较低,长8原油饱/芳比值较高,说明长6原油和长8原油不同源。长7烃源岩与长9烃源岩在生物标志化合物特征上有明显区别。规则甾烷C27-C28-C29αααR指纹分布样式上,长7呈现"L"型,长9呈现偏"V"型与反"L"型,长8原油呈现偏"V"型分布。研究区长8原油主要来源于长9烃源岩。 相似文献
11.
从滴南凸起10个含油储集岩样品分步提取了自由态油气组分、束缚态油气组分和油气包裹体组分,各组分进一步做色谱、色谱-质谱和正构烷烃单体碳同位素分析。根据生物标志物组成,可将10个含油储集岩样分为两类：第一类包括D2-1和D18-12个侏罗系油砂样,第二类包括其他8个采自侏罗系、二叠系和石炭系含油储集岩样。两类样品生物标志物组成差异主要有：（1）第一类样品各类油气组分三环萜烷含量明显低于第二类样品;（2）第一类样品 C20、C21和 C23三环萜烷含量比较接近,其分布模式为 C20＆lt;C21＆gt;C23,第二类样品这3个化合物含量差异较大,且分布模式为C20＆gt;C21＆gt;C23;（3）第一类样品伽马蜡烷和β-胡萝卜烷相对含量高于第二类样品;（4）第一类样品C27甾烷含量较低而C28甾烷含量较高,第二类样品则相反。可以推断第一类样品自由态组分、束缚态组分和油气包裹体均来源于二叠系烃源岩而第二类样品各类油气组分则来源于石炭系烃源岩。第一类样品油气包裹体成熟度明显高于自由态组分和束缚态组分,表明早期充注原油的成熟度高于晚期充注的原油,总体上各类油气组分成熟度位于生油高峰阶段（Ro 0.8%~1.1%）。第二类样品从自由态组分、束缚态组分至油气包裹体成熟度依次降低,表明早期充注原油的成熟度低于晚期充注的原油,总体上各类油气组分成熟度位于高-过成熟阶段（Ro〉1.25%）。第一类样品各类油气组分正构烷烃单体碳同位素组成相对较轻,第二类样品各类油气组分正构烷烃单体碳同位素组成有一定的差异,组成较轻者与第一类样品各类油气组分接近。 相似文献
12.
The present paper deals with the biomarker characteristics of crude oils and source rocks from different environments(fresh,fresh-brackish and salt waters)of nonmarine depositional basins of different ages in China.Their characters are summarized as follows:1)Souce rocks and crude oils derived from fresh-water lacustrine facies have an odd/even predominance of n-alkanes and high pristine/phytane ratios.Oils from the fresh-water lacustrine facies differ from typical marine oils in the relative contents of total steranes and terpanes,the concentrations of hopanes and organic sul-phur compounds and the values of methylphenanthrene indices and C,H,S stable isotopes.2)The source rocks and crude oils derived from saline lacustrine facies possess an even/odd predominance of n-alkanes and high phytane/pristine ratios.There are also some differences between saline lacustrine oils and freshwater lacustrine oils in the concentrations of steranes,tricyclic terpanes and organic sulphur compounds,as well as in the values of methylphenanthrene indices and C,H,S stable isotopes.3)Oils derived from fresh-brackish water lake facies differ from oils from fresh-water lacustrine or samline lacustrine environments in respect of some biomarkers.According to the various distributions of these biomarkers,a number of geochemical parameters can be applied synthetically to differentiating and identifying the nature of original depositional environments of crude oils and source rocks and that of organisms-primary source materials present in those environments. 相似文献
13.
Yangming Zhu 《中国地球化学学报》2001,20(1):73-87
Based on the compositions and distributions of biomarkers in thirty-five representative oil samples, oils from the Tarim Basin of northwestern China are mainly divided into two oil families. One oil family contains relatively low amounts of C15-C20 isoprenoid hydrocarbons and shows pristane predominance with Pr/Ph ratios ranging from 1.50 to 3.00. The GC/MS analytical data of these oils show the occurrence of abundant hopanes, and low concentrations of steranes and tricyclic terpanes with hopanes/steranes ratios from 6.25 to 12.24 and tricyclic terpanes/hopanes ratios from 0.03 to 0.24. These oils contain low drimane relative to homodrimane (C15/C16 < 1.0) and abundant rearranged bicyclanes in bicyclic sesquiterpanes. They are dominated by low carbon number (C19-C21) compounds in the tricyclic terpanes, and are rich in rearranged hopanes, C29Ts and an unknown C30 compound in pentacyclic triterpanes. These geochemical characteristics suggest that the oils were generated mainly from terrigenous organic matter. The other oil family shows remarkably different biomarker compositions and distributions. The oils revealed Pr/Ph ratios of about 1.0, high drimane/homodrimane ratios (>1.0), low hopanes/steranes ratios (0.65–2.50), high tricyclic terpanes/hopanes ratios (0.30–2.00) and a dominant peak at C23 in tricyclic tepanes, suggesting a marine organic origin. Oil-source rock correlation indicates that these two oil families seem to have been derived from Mesozoic Jurassic-Triassic terrestrial source rocks (shales and coal seams) and Lower Paleozoic Ordovician-Cambrian marine source rocks, respectively. 相似文献
14.
各类生物标志物的组成特征表明:柴达木盆地北缘的冷湖油田原油具有姥植比高（Pr/Ph>2.0）,重排甾烷（C27重排甾烷/规则甾烷=0.5~0.7）、重排藿烷（diaC30H/C30H=0.2~0.4）和新藿烷（C29Ts/C29H=0.4~0.7）含量中等,伽马蜡烷含量低（伽马蜡烷指数<0.05）的特征,它们源于该地区发育的下侏罗统淡水湖沼相烃源岩;而柴西北区咸水湖相原油的姥植比低（Pr/Ph<0.8）,重排甾烷（C27重排甾烷/规则甾烷<0.1）、重排藿烷（diaC30H/C30H<0.05）和新藿烷（C29Ts/C29H=0.2~0.4）含量低和伽马蜡烷含量高（伽马蜡烷指数=0.4~0.8）,这一系列特征与柴西地区发育的古近系-新近系咸水湖相烃源岩一致。但是,东坪地区原油呈现完全不同的生物标志物组合,主要表现为丰富的伽马蜡烷（伽马蜡烷指数=1.2~3.0）与高含量的新藿烷（C29Ts/C29H>1.5）、重排藿烷（diaC30H/C30H>0.7）和重排甾烷（C27重排甾烷/规则甾烷>0.4）并存,这与地质样品中伽马蜡烷和重排类标志物的分布特征相矛盾,因为依据现有的认识无法解释这一特殊地球化学现象。生物标志物组成特征表明东坪地区原油所具有的特殊生物标志物组合并非源于不同类型原油之间的混合,而是一种客观存在,尽管其确切的地球化学意义和形成条件目前并不清楚。由此可见,东坪地区原油为柴达木盆地一个新的原油类型,推测其烃源岩可能形成于偏酸性的咸水环境。 相似文献
15.
利用芳烃参数研究煤系烃源岩中重排藿烷成因 总被引：4，自引：1，他引：3
研究发现鄂尔多斯盆地部分地区上古生界煤系烃源岩存在较高丰度的17α(H)-重排藿烷和早洗脱重排藿烷,在对重排藿烷分布、组成特征及生标组成特征研究的基础上,应用芳烃参数对高丰度重排藿烷的成因进行了探讨。饱和烃生物标志物组成特征显示,高重排藿烷与陆源高等植物生源关系密切,主要在弱氧化沉积环境下演化形成。具有高-异常高丰度17α(H)-重排藿烷和早洗脱重排藿烷(C30*/C30H>0.2、C30E/C30H>0.1)的烃源岩二环+三环芳烃相对含量一般大于50%,四环、五环芳烃含量相对较低,普遍低于35%,未见芳香甾萜类,研究认为其生源主要为陆生高等植物;甲基菲指数MPI1、MPI2和甲基菲比值F1研究结果显示,Pr/Ph>1的弱氧化环境烃源岩17α(H)-重排藿烷和早洗脱重排藿烷在进入成熟阶段后开始大量形成,并随成熟度升高而增大;Pr/Ph<1还原环境下的烃源岩重排藿烷丰度相对较低,但在进入成熟阶段后仍有随成熟度升高而增大的趋势;三芴系列化合物参数表明,沉积环境的弱氧化性质对17α(H)-重排藿烷和早洗脱重排藿烷的形成有较大的影响,沼泽相沉积环境最有利于重排藿烷的形成。 相似文献
16.
Origin and occurrence of 25-norhopanes: a statistical study 总被引：1，自引：0，他引：1
The alkane fraction of more than 200 rocks, biodegraded oils and non-biodegraded oils, have been analysed by means of computerized GC-MS, in order to investigate the effect of natural biodegradation on the occurrence of “demethylated hopanes”, i.e. 17α-25-norhopanes. The results obtained indicate that 25-norhopanes are preexisting biomarkers the concentration of which is enhanced by selective biodegradation of more readily degradable homologs, i.e. regular hopanes, rather than by demethylation of hopanes in reservoirs. However, the use of 25-norhopane enrichment as a palaebiodegradation indicator in apparently non-biodegraded oils is still valuable providing the initial background content in the corresponding source rocks is known. Furthermore, 25-norhopanes appear to be diagnostic of specific environmental conditions (marine and lacustrine source rocks, dysoxic and not very hypersaline). Lastly, one other (novel) bacterially resistant rearranged hopanoic compound, namely a C29 neohopane, is applicable for both biodegradation and maturation evaluation. 相似文献
17.
PAUL Philp 《中国地球化学学报》2012,31(3):264-275
Based on the systematic analyses of fifteen typical crude oils and ten typical potential source rocks col-lected from the Qaidam,Tarim and Turpan basins,Northwest China,the geochemical characteristics of the oils and source rocks were investigated and oil-source rock correlations undertaken.The oils and source rocks deposited in saline lacustrine environment from the western Qaidam Basin were characterized by n-alkanes with even car-bon-number preference in the C20-C28 range,low pristane/phytane(Pr/Ph) ratios(less than 0.5),and high abundances of C27 steranes,gammacerane and C35 hopanes.The oils and source rocks deposited in marine environment from the Tarim Basin were characterized by n-alkanes with even carbon-number preference in the C14-C18 range,relatively low Pr/Ph ratios(near to 1),high abundance of C28 steranes,and relatively high gammacerane.In contrast,the oils and source rocks deposited in terrigenous bog environment from the Turpan Basin were characterized by relatively high Pr/Ph ratios(oil samples greater than 6) high abundance of C29 steranes,and relatively low gammacerane and C31-35 hopanes.The higher amounts of C37 and C38 n-alkanes of source rocks from the western Qaidam Basin and the Tarim Basin suggest an origin of these alkanes from functionalized C37 and C38 n-alkadienes and alkenones in prymnesiophytes living in lacustrine and marine environments.Oil-source rock correlations suggest oils in the west-ern Qaidam Basin were derived from the Oligocene Lower Ganchaigou Formation(E3),oils in the Tabei and Tazhong uplifts from the Tarim Basin have a genetic relationship with the Middle-Upper Ordovician source beds.Oils in the Turpan Basin generally fall into two genetic types.Most oils in the Taibei depression from the Turpan Basin were derived from the Lower-Middle Jurassic coal measures,but the fewer oils in this region are a mixed source derived from the Lower-Middle Jurassic coal measure and the Upper Permian source rocks. 相似文献
18.
Hans Peter Nytoft 《Organic Geochemistry》2011,42(5):520-539
Novel side chain methylated and hexacyclic hopanes have been identified in coals and oils from around the world. Extended hopanes (>C32) with an additional methyl in the side chain (“isohopanes”) were identified by comparison with synthetic standards. The major C33-C35 isohopanes are 31-methylbishomohopanes, 32-methyltrishomohopanes and 33-methyltetrakishomohopanes. Extended hopanes methylated at C-29 were not detected. The 17α(H),21β(H)-31-methyltrishomohopanes show four peaks on gas chromatography because of the extra asymmetric carbon at C-31. Like regular hopanes, the isohopanes extend beyond C35. Low concentrations of novel hexacyclic hopanes having 35 or more carbons were also detected in oils and coal extracts. The C35 hexacyclic hopanes were identified as 29-cyclopentylhopanes. Isohopanes are released from the kerogen by hydrous pyrolysis and hydropyrolysis. The 22S/(22S + 22R) ratio for 31-methylbishomohopanes and other isohopanes is around 0.60 at equilibrium in geological samples. They isomerize slightly more slowly than regular C33 hopanes. Isohop-17(21)-enes, 2α-methylisohopanes and two series of rearranged isohopanes were tentatively identified. Isohopanes can be biodegraded to form the corresponding 25-norhopanes. When 25-norhopanes are not formed, the isohopanes are much more resistant to biodegradation than regular hopanes. In biodegraded oil seeps from Greece, 30-norisohopanes were tentatively assigned. The composition and relative abundance of C33 and C34 isohopanes in a worldwide set of coals and crude oils was determined. Isohopanes are abundant in coal and coal-generated oils, where they can account for more than 5% of all extended hopanes, and low in abundance in oils from source rocks deposited under anoxic conditions. 相似文献
19.
China has a number of petroliferous lacustrine sedimentary basins of varying salinity and age (mainly Eocene). A geochemical investigation has been undertaken on several oils and source rocks from the Eocene lacustrine Biyang Basin. The distributions of n-alkanes, isoprenoids, steranes, and terpanes have been studied and used to characterize the sedimentary environment of deposition, maturity, biodegradation and undertake possible correlations. The ratios of C30-hopane/gammacerane, 4-methyl-steranes/regular steranes, steranes/hopanes, C21 tricyclic/C30 hopane are proposed to be indicative of the depositional environment whereas ß-carotane appears to be a source related indicator. The geochemical data obtained in this study suggest that the major source rocks in the Biyang Basin were deposited in a saline/hypersaline depositional environment. 相似文献